A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155883



Internal ID22086388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:173039535..173045842hg38UCSC Ensembl
Outerchr2:173039072..173047192hg38UCSC Ensembl
Innerchr2:173904263..173910570hg19UCSC Ensembl
Outerchr2:173903800..173911920hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg388121
hg198121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015307
Samples
Known GenesRAPGEF4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155883
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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